Alloxazine;Isoalloxazine structure
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Common Name | Alloxazine;Isoalloxazine | ||
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CAS Number | 490-59-5 | Molecular Weight | 214.18000 | |
Density | 1.509g/cm3 | Boiling Point | N/A | |
Molecular Formula | C10H6N4O2 | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of Alloxazine;IsoalloxazineAlloxazine is a selective A2b antagonist. Alloxazine can completely block 5’N-Ethylcarboxamido adenosine (NECA)-mediated cyclic AMP accumulation with an IC50 of 2.9 μM. Alloxazine can be used for the research of cancer[1][2]. |
Name | alloxazine |
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Synonym | More Synonyms |
Description | Alloxazine is a selective A2b antagonist. Alloxazine can completely block 5’N-Ethylcarboxamido adenosine (NECA)-mediated cyclic AMP accumulation with an IC50 of 2.9 μM. Alloxazine can be used for the research of cancer[1][2]. |
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Related Catalog | |
Target |
IC50: 2.9 μM (AMP)[1] |
In Vitro | Alloxazine (0-30 μM, 20 min) inhibits cyclic AMP production in PGT-β cells[1]. Cell Viability Assay[1] Cell Line: PGT-β cells Concentration: 0-30 μM Incubation Time: 20 min Result: Inhibited the cyclic AMP generation concentration-dependently with an IC IC50 of 2.9 μM. |
In Vivo | Alloxazine (1 µmol/L, 0-20 min) suppresses NECA-induced vasodilation[2]. Animal Model: 250–320 g male Sprague-Dawley rats[2] Dosage: 1 µmol/L Administration: Cortical surface suffusion; 1 µmol/L once Result: Significantly suppressed vasodilation with increased EC25 value of 0.60 µmol/L. |
References |
Density | 1.509g/cm3 |
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Molecular Formula | C10H6N4O2 |
Molecular Weight | 214.18000 |
Exact Mass | 214.04900 |
PSA | 91.50000 |
LogP | 0.15960 |
Index of Refraction | 1.699 |
Storage condition | -20℃ |
WGK Germany | 3 |
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HS Code | 2933990090 |
HS Code | 2933990090 |
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Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
Alloxazin |
1H-benzo[g]pteridine-2,4-dione |
Alloxazine |